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Journal Abstract Search

245 related items for PubMed ID: 36130307

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  • 22. The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria.
    Ojewunmi OO, Adeyemo TA, Oyetunji AI, Inyang B, Akinrindoye A, Mkumbe BS, Gardner K, Rooks H, Brewin J, Patel H, Lee SH, Chung R, Rashkin S, Kang G, Chianumba R, Sangeda R, Mwita L, Isa H, Agumadu UN, Ekong R, Faruk JA, Jamoh BY, Adebiyi NM, Umar IA, Hassan A, Grace C, Goel A, Inusa BPD, Falchi M, Nkya S, Makani J, Ahmad HR, Nnodu O, Strouboulis J, Menzel S.
    Hum Mol Genet; 2024 May 04; 33(10):919-929. PubMed ID: 38339995
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  • 31. The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes.
    Jiang Z, Luo HY, Huang S, Farrell JJ, Davis L, Théberge R, Benson KA, Riolueang S, Viprakasit V, Al-Allawi NA, Ünal S, Gümrük F, Akar N, Başak AN, Osorio L, Badens C, Pissard S, Joly P, Campbell AD, Gallagher PG, Steinberg MH, Forget BG, Chui DH.
    Br J Haematol; 2016 Mar 04; 172(6):958-65. PubMed ID: 26771086
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  • 32. Correlations between Multiple SNPs and HbF Levels in β-Thalassemia Carriers.
    Xu Q, Huang L, Jin T, Han Y, Liu J, Zhang W, Biao Y, An B, Huang S.
    Clin Lab; 2023 Sep 01; 69(9):. PubMed ID: 37702677
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  • 34. Genetic variants associated with fetal hemoglobin levels show the diverse ethnic origin in Colombian patients with sickle cell anemia.
    Fong C, Menzel S, Lizarralde MA, Barreto G.
    Biomedica; 2015 Sep 01; 35(3):437-43. PubMed ID: 26849705
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  • 36. Influence of BCL11A, HBS1L-MYB, HBBP1 single nucleotide polymorphisms and the HBG2 XmnI polymorphism On Hb F levels.
    Roy P, Bhattacharya G, Mandal A, Dasgupta UB, Banerjee D, Chandra S, Das M.
    Hemoglobin; 2012 Sep 01; 36(6):592-9. PubMed ID: 23094636
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